Immortalized Human Dorsal Root Ganglion Cells Differentiate into Neurons with Nociceptive Properties
A renewable source of human sensory neurons would greatly facilitate basic research and drug development. We had established previously conditionally immortalized human CNS cell lines that can differentiate into functional neurons (). We report here the development of an immortalized human dorsal ro...
Gespeichert in:
Veröffentlicht in: | The Journal of neuroscience 1999-07, Vol.19 (13), p.5420-5428 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 5428 |
---|---|
container_issue | 13 |
container_start_page | 5420 |
container_title | The Journal of neuroscience |
container_volume | 19 |
creator | Raymon, Heather K Thode, Silke Zhou, Jiuying Friedman, Glenn C Pardinas, Jose R Barrere, Christian Johnson, Randolph M Sah, Dinah W. Y |
description | A renewable source of human sensory neurons would greatly facilitate basic research and drug development. We had established previously conditionally immortalized human CNS cell lines that can differentiate into functional neurons (). We report here the development of an immortalized human dorsal root ganglion (DRG) clonal cell line, HD10.6, with a tetracycline-regulatable v-myc oncogene. In the proliferative condition, HD10.6 cells have a doubling time of 1.2 d and exhibit a neuronal precursor morphology. After differentiation of clone HD10.6 for 7 d in the presence of tetracycline, v-myc expression was suppressed, and >50% of the cells exhibited typical neuronal morphology, stained positively for neuronal cytoskeletal markers, and fired action potentials in response to current injection. Furthermore, this cell line was fate-restricted to a neuronal phenotype; even in culture conditions that promote Schwann cell or smooth muscle differentiation of neural crest stem cells, HD10.6 differentiated exclusively into neurons. Moreover, differentiated HD10.6 cells expressed sensory neuron-associated transcription factors and exhibited capsaicin sensitivity. Taken together, these data indicate that we have established an immortalized human DRG cell line that can differentiate into sensory neurons with nociceptive properties. The cell line HD10.6 represents the first example of a human sensory neuronal line and will be valuable for basic research, as well as for the discovery of novel drug targets and clinical candidates. |
doi_str_mv | 10.1523/jneurosci.19-13-05420.1999 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6782307</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69837251</sourcerecordid><originalsourceid>FETCH-LOGICAL-c542t-81631e891da6ae8f671a5c8ee8c3115b2538cc59d1d8040805507d76419a9d533</originalsourceid><addsrcrecordid>eNqFkUFv1DAUhC0EokvhLyCLA5xS_OI4tjkgoW1pF1VbVOjZcp2XXVdJvNjZRvDr8ZIKlROnd3jfjGY0hLwBdgKi5O_vBtzHkJw_AV0AL5ioyvzSWj8hi0zooqwYPCULVkpW1JWsjsiLlO4YY5KBfE6OgHEpuYAFaVZ9H-JoO_8LG3qx7-1AT0NMtqPXIYz03A6bzoeBLrHrEj31bYsRh9HbEakfxkDXhzBDopMft3QdnHe4G_090q8x7DCOHtNL8qy1XcJXD_eY3Hw--768KC6vzlfLT5eFyw3GQkHNAZWGxtYWVVtLsMIpROU4gLgtBVfOCd1Ao1jFFBOCyUbWFWirG8H5Mfk4--72tz02LueMtjO76Hsbf5pgvfn3M_it2YR7U0tVciazwdsHgxh-7DGNpvfJ5eZ2wLBPptaKy1LAf0GQpZSsrDP4YQZdXixFbP-mAWYOa5ov67Ob66tvy5UBbYCbP2uaw5pZ_Ppxn0fSeb4MvJuBrd9sJx_RpN52XcbBTNM0Gx78-G_-Xaz1</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17277026</pqid></control><display><type>article</type><title>Immortalized Human Dorsal Root Ganglion Cells Differentiate into Neurons with Nociceptive Properties</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Raymon, Heather K ; Thode, Silke ; Zhou, Jiuying ; Friedman, Glenn C ; Pardinas, Jose R ; Barrere, Christian ; Johnson, Randolph M ; Sah, Dinah W. Y</creator><creatorcontrib>Raymon, Heather K ; Thode, Silke ; Zhou, Jiuying ; Friedman, Glenn C ; Pardinas, Jose R ; Barrere, Christian ; Johnson, Randolph M ; Sah, Dinah W. Y</creatorcontrib><description>A renewable source of human sensory neurons would greatly facilitate basic research and drug development. We had established previously conditionally immortalized human CNS cell lines that can differentiate into functional neurons (). We report here the development of an immortalized human dorsal root ganglion (DRG) clonal cell line, HD10.6, with a tetracycline-regulatable v-myc oncogene. In the proliferative condition, HD10.6 cells have a doubling time of 1.2 d and exhibit a neuronal precursor morphology. After differentiation of clone HD10.6 for 7 d in the presence of tetracycline, v-myc expression was suppressed, and >50% of the cells exhibited typical neuronal morphology, stained positively for neuronal cytoskeletal markers, and fired action potentials in response to current injection. Furthermore, this cell line was fate-restricted to a neuronal phenotype; even in culture conditions that promote Schwann cell or smooth muscle differentiation of neural crest stem cells, HD10.6 differentiated exclusively into neurons. Moreover, differentiated HD10.6 cells expressed sensory neuron-associated transcription factors and exhibited capsaicin sensitivity. Taken together, these data indicate that we have established an immortalized human DRG cell line that can differentiate into sensory neurons with nociceptive properties. The cell line HD10.6 represents the first example of a human sensory neuronal line and will be valuable for basic research, as well as for the discovery of novel drug targets and clinical candidates.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/jneurosci.19-13-05420.1999</identifier><identifier>PMID: 10377351</identifier><language>eng</language><publisher>United States: Soc Neuroscience</publisher><subject>Action Potentials ; Capsaicin - pharmacology ; Cations - metabolism ; Cell Differentiation ; Cell Line ; Cell Lineage ; Cell Size ; Clone Cells - cytology ; Clone Cells - drug effects ; Clone Cells - metabolism ; Ganglia, Spinal - cytology ; Ganglia, Spinal - embryology ; Genes, myc - genetics ; Humans ; Ion Channel Gating ; Ligands ; Neurons, Afferent - cytology ; Neurons, Afferent - drug effects ; Neurons, Afferent - metabolism ; Neurons, Afferent - physiology ; Nociceptors - physiology ; Pain ; Stem Cells - cytology ; Stem Cells - drug effects ; Stem Cells - metabolism ; Tetracycline - pharmacology ; Transcription Factors - analysis</subject><ispartof>The Journal of neuroscience, 1999-07, Vol.19 (13), p.5420-5428</ispartof><rights>Copyright © 1999 Society for Neuroscience 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c542t-81631e891da6ae8f671a5c8ee8c3115b2538cc59d1d8040805507d76419a9d533</citedby><cites>FETCH-LOGICAL-c542t-81631e891da6ae8f671a5c8ee8c3115b2538cc59d1d8040805507d76419a9d533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782307/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782307/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10377351$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raymon, Heather K</creatorcontrib><creatorcontrib>Thode, Silke</creatorcontrib><creatorcontrib>Zhou, Jiuying</creatorcontrib><creatorcontrib>Friedman, Glenn C</creatorcontrib><creatorcontrib>Pardinas, Jose R</creatorcontrib><creatorcontrib>Barrere, Christian</creatorcontrib><creatorcontrib>Johnson, Randolph M</creatorcontrib><creatorcontrib>Sah, Dinah W. Y</creatorcontrib><title>Immortalized Human Dorsal Root Ganglion Cells Differentiate into Neurons with Nociceptive Properties</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>A renewable source of human sensory neurons would greatly facilitate basic research and drug development. We had established previously conditionally immortalized human CNS cell lines that can differentiate into functional neurons (). We report here the development of an immortalized human dorsal root ganglion (DRG) clonal cell line, HD10.6, with a tetracycline-regulatable v-myc oncogene. In the proliferative condition, HD10.6 cells have a doubling time of 1.2 d and exhibit a neuronal precursor morphology. After differentiation of clone HD10.6 for 7 d in the presence of tetracycline, v-myc expression was suppressed, and >50% of the cells exhibited typical neuronal morphology, stained positively for neuronal cytoskeletal markers, and fired action potentials in response to current injection. Furthermore, this cell line was fate-restricted to a neuronal phenotype; even in culture conditions that promote Schwann cell or smooth muscle differentiation of neural crest stem cells, HD10.6 differentiated exclusively into neurons. Moreover, differentiated HD10.6 cells expressed sensory neuron-associated transcription factors and exhibited capsaicin sensitivity. Taken together, these data indicate that we have established an immortalized human DRG cell line that can differentiate into sensory neurons with nociceptive properties. The cell line HD10.6 represents the first example of a human sensory neuronal line and will be valuable for basic research, as well as for the discovery of novel drug targets and clinical candidates.</description><subject>Action Potentials</subject><subject>Capsaicin - pharmacology</subject><subject>Cations - metabolism</subject><subject>Cell Differentiation</subject><subject>Cell Line</subject><subject>Cell Lineage</subject><subject>Cell Size</subject><subject>Clone Cells - cytology</subject><subject>Clone Cells - drug effects</subject><subject>Clone Cells - metabolism</subject><subject>Ganglia, Spinal - cytology</subject><subject>Ganglia, Spinal - embryology</subject><subject>Genes, myc - genetics</subject><subject>Humans</subject><subject>Ion Channel Gating</subject><subject>Ligands</subject><subject>Neurons, Afferent - cytology</subject><subject>Neurons, Afferent - drug effects</subject><subject>Neurons, Afferent - metabolism</subject><subject>Neurons, Afferent - physiology</subject><subject>Nociceptors - physiology</subject><subject>Pain</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - drug effects</subject><subject>Stem Cells - metabolism</subject><subject>Tetracycline - pharmacology</subject><subject>Transcription Factors - analysis</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAUhC0EokvhLyCLA5xS_OI4tjkgoW1pF1VbVOjZcp2XXVdJvNjZRvDr8ZIKlROnd3jfjGY0hLwBdgKi5O_vBtzHkJw_AV0AL5ioyvzSWj8hi0zooqwYPCULVkpW1JWsjsiLlO4YY5KBfE6OgHEpuYAFaVZ9H-JoO_8LG3qx7-1AT0NMtqPXIYz03A6bzoeBLrHrEj31bYsRh9HbEakfxkDXhzBDopMft3QdnHe4G_090q8x7DCOHtNL8qy1XcJXD_eY3Hw--768KC6vzlfLT5eFyw3GQkHNAZWGxtYWVVtLsMIpROU4gLgtBVfOCd1Ao1jFFBOCyUbWFWirG8H5Mfk4--72tz02LueMtjO76Hsbf5pgvfn3M_it2YR7U0tVciazwdsHgxh-7DGNpvfJ5eZ2wLBPptaKy1LAf0GQpZSsrDP4YQZdXixFbP-mAWYOa5ov67Ob66tvy5UBbYCbP2uaw5pZ_Ppxn0fSeb4MvJuBrd9sJx_RpN52XcbBTNM0Gx78-G_-Xaz1</recordid><startdate>19990701</startdate><enddate>19990701</enddate><creator>Raymon, Heather K</creator><creator>Thode, Silke</creator><creator>Zhou, Jiuying</creator><creator>Friedman, Glenn C</creator><creator>Pardinas, Jose R</creator><creator>Barrere, Christian</creator><creator>Johnson, Randolph M</creator><creator>Sah, Dinah W. Y</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19990701</creationdate><title>Immortalized Human Dorsal Root Ganglion Cells Differentiate into Neurons with Nociceptive Properties</title><author>Raymon, Heather K ; Thode, Silke ; Zhou, Jiuying ; Friedman, Glenn C ; Pardinas, Jose R ; Barrere, Christian ; Johnson, Randolph M ; Sah, Dinah W. Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c542t-81631e891da6ae8f671a5c8ee8c3115b2538cc59d1d8040805507d76419a9d533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Action Potentials</topic><topic>Capsaicin - pharmacology</topic><topic>Cations - metabolism</topic><topic>Cell Differentiation</topic><topic>Cell Line</topic><topic>Cell Lineage</topic><topic>Cell Size</topic><topic>Clone Cells - cytology</topic><topic>Clone Cells - drug effects</topic><topic>Clone Cells - metabolism</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Spinal - embryology</topic><topic>Genes, myc - genetics</topic><topic>Humans</topic><topic>Ion Channel Gating</topic><topic>Ligands</topic><topic>Neurons, Afferent - cytology</topic><topic>Neurons, Afferent - drug effects</topic><topic>Neurons, Afferent - metabolism</topic><topic>Neurons, Afferent - physiology</topic><topic>Nociceptors - physiology</topic><topic>Pain</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - drug effects</topic><topic>Stem Cells - metabolism</topic><topic>Tetracycline - pharmacology</topic><topic>Transcription Factors - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raymon, Heather K</creatorcontrib><creatorcontrib>Thode, Silke</creatorcontrib><creatorcontrib>Zhou, Jiuying</creatorcontrib><creatorcontrib>Friedman, Glenn C</creatorcontrib><creatorcontrib>Pardinas, Jose R</creatorcontrib><creatorcontrib>Barrere, Christian</creatorcontrib><creatorcontrib>Johnson, Randolph M</creatorcontrib><creatorcontrib>Sah, Dinah W. Y</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raymon, Heather K</au><au>Thode, Silke</au><au>Zhou, Jiuying</au><au>Friedman, Glenn C</au><au>Pardinas, Jose R</au><au>Barrere, Christian</au><au>Johnson, Randolph M</au><au>Sah, Dinah W. Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immortalized Human Dorsal Root Ganglion Cells Differentiate into Neurons with Nociceptive Properties</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>1999-07-01</date><risdate>1999</risdate><volume>19</volume><issue>13</issue><spage>5420</spage><epage>5428</epage><pages>5420-5428</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>A renewable source of human sensory neurons would greatly facilitate basic research and drug development. We had established previously conditionally immortalized human CNS cell lines that can differentiate into functional neurons (). We report here the development of an immortalized human dorsal root ganglion (DRG) clonal cell line, HD10.6, with a tetracycline-regulatable v-myc oncogene. In the proliferative condition, HD10.6 cells have a doubling time of 1.2 d and exhibit a neuronal precursor morphology. After differentiation of clone HD10.6 for 7 d in the presence of tetracycline, v-myc expression was suppressed, and >50% of the cells exhibited typical neuronal morphology, stained positively for neuronal cytoskeletal markers, and fired action potentials in response to current injection. Furthermore, this cell line was fate-restricted to a neuronal phenotype; even in culture conditions that promote Schwann cell or smooth muscle differentiation of neural crest stem cells, HD10.6 differentiated exclusively into neurons. Moreover, differentiated HD10.6 cells expressed sensory neuron-associated transcription factors and exhibited capsaicin sensitivity. Taken together, these data indicate that we have established an immortalized human DRG cell line that can differentiate into sensory neurons with nociceptive properties. The cell line HD10.6 represents the first example of a human sensory neuronal line and will be valuable for basic research, as well as for the discovery of novel drug targets and clinical candidates.</abstract><cop>United States</cop><pub>Soc Neuroscience</pub><pmid>10377351</pmid><doi>10.1523/jneurosci.19-13-05420.1999</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0270-6474 |
ispartof | The Journal of neuroscience, 1999-07, Vol.19 (13), p.5420-5428 |
issn | 0270-6474 1529-2401 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6782307 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Action Potentials Capsaicin - pharmacology Cations - metabolism Cell Differentiation Cell Line Cell Lineage Cell Size Clone Cells - cytology Clone Cells - drug effects Clone Cells - metabolism Ganglia, Spinal - cytology Ganglia, Spinal - embryology Genes, myc - genetics Humans Ion Channel Gating Ligands Neurons, Afferent - cytology Neurons, Afferent - drug effects Neurons, Afferent - metabolism Neurons, Afferent - physiology Nociceptors - physiology Pain Stem Cells - cytology Stem Cells - drug effects Stem Cells - metabolism Tetracycline - pharmacology Transcription Factors - analysis |
title | Immortalized Human Dorsal Root Ganglion Cells Differentiate into Neurons with Nociceptive Properties |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T23%3A17%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immortalized%20Human%20Dorsal%20Root%20Ganglion%20Cells%20Differentiate%20into%20Neurons%20with%20Nociceptive%20Properties&rft.jtitle=The%20Journal%20of%20neuroscience&rft.au=Raymon,%20Heather%20K&rft.date=1999-07-01&rft.volume=19&rft.issue=13&rft.spage=5420&rft.epage=5428&rft.pages=5420-5428&rft.issn=0270-6474&rft.eissn=1529-2401&rft_id=info:doi/10.1523/jneurosci.19-13-05420.1999&rft_dat=%3Cproquest_pubme%3E69837251%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17277026&rft_id=info:pmid/10377351&rfr_iscdi=true |